A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6329736



Internal ID9307139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70839253..70843001hg38UCSC Ensembl
chr10:72599010..72602758hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383749
hg193749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665625
Supporting Variants
SamplesNA12778
Known GenesSGPL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6329736
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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